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Usp15L749R
Chemically induced Allele Detail
Summary
Symbol: Usp15L749R
Name: ubiquitin specific peptidase 15; L749R
MGI ID: MGI:6149704
Gene: Usp15  Location: Chr10:122940911-123032900 bp, - strand  Genetic Position: Chr10, 72.31 cM, cytoband D3
Alliance: Usp15L749R page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to G point mutation in exon 17 that produces an amino acid substitution of leucine with arginine at position 749 (L749R). (J:259382)
Inheritance:    Other (see notes)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Usp15 Mutation:  60 strains or lines available
Notes
This allele is inherited in an ncompletely recessive mode.
References
Original:  J:259382 Torre S, et al., USP15 regulates type I interferon response and is required for pathogenesis of neuroinflammation. Nat Immunol. 2017 Jan;18(1):54-63
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory